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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222135Generated: October 31, 2026

3,5-Dimethylpiperidine → 3-Methylthio-5-(3,5-dimethylpiperidino)-1,2,4-thiadiazole

https://huagongshe.com/reaction/2222135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylpiperidineHCID 118259—
Reactant5-Chloro-3-(methylsulfanyl)-1,2,4-thiadiazoleHCID 570953—
SolventDimethylformamideHCID 6228—
Solventtert-Butyl methyl etherHCID 15413—
Product3-Methylthio-5-(3,5-dimethylpiperidino)-1,2,4-thiadiazoleHCID 5879211079.6%

Reaction Steps

In 9 ml of N,N-dimethylformamide was dissolved 740 mg of 5-chloro-3-methylthio-1,2,4-thiadiazole, and 1.25 g of 3,5-dimethylpiperidine (a mixture of 8:2 geometrical isomers) was added dropwise under ice-cooling. The mixture was stirred at room temperature for 20 minutes. The reaction mixture was diluted with tert-butyl methyl ether, and extracted with tert-butyl methyl ether after the addition of 10% hydrochloric acid. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 860 mg of 3-methylthio-5-(3,5-dimethylpiperidino)-1,2,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371746B2
Source datasetuspto-grants-2008_05
ORD IDord-e0be2c8dfbad412186455aaf7077029d
Source noteuspto-grants-2008_05